Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the tarsal bones (HP:0001850)help
Grandparent Node:
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Synostosis involving bones of the feet (HP:0009140)help
Grandparent Node:
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Synostosis of carpals/tarsals (HP:0100266)help
Parent Node:
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Tarsal synostosis (HP:0008368)help
..Starting node
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Coalescence of tarsal bones (HP:0005802)help
Term ID: 5802
Name: Coalescence of tarsal bones
Synonym:
Definition:
Comments:
Reference: HP:0005802
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCalcaneonavicular fusion (HP:0008122) help
..expandPartial fusion of tarsals (HP:0008097) help
..expandTalocalcaneal synostosis (HP:0005682) help
..expandTarsometatarsal synostosis (HP:0100329) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005802HP:0005802Coalescence of tarsal bones0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.